Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yu Seiki"'
Autor:
Yu Seiki, Yumi Sasaki, Kohei Hosokawa, Chizuru Saito, Naomi Sugimori, Hirohito Yamazaki, Akiyoshi Takami, Shinji Nakao
Publikováno v:
Haematologica, Vol 98, Iss 6 (2013)
Although myelodysplastic syndromes are heterogeneous disorders comprising a benign subset of bone marrow failure similar to aplastic anemia, no laboratory test has been established to distinguish it from bone marrow failures that can evolve into acut
Externí odkaz:
https://doaj.org/article/964a80aa582c425c87325104b834c051
Autor:
Kohei Hosokawa, Takamasa Katagiri, Naomi Sugimori, Ken Ishiyama, Yumi Sasaki, Yu Seiki, Aiko Sato-Otsubo, Masashi Sanada, Seishi Ogawa, Shinji Nakao
Publikováno v:
Haematologica, Vol 97, Iss 12 (2012)
To characterize bone marrow failure with del(13q), we reviewed clinical records of 22 bone marrow failure patients possessing del(13q) alone or del(13q) plus other abnormalities. All del(13q) patients were diagnosed with myelodysplastic syndrome-uncl
Externí odkaz:
https://doaj.org/article/dd901f4df73342ac9c2cb0d29d706f84
Autor:
Akiyoshi Takami, Naomi Sugimori, Kohei Hosokawa, Yumi Sasaki, Takamasa Katagiri, Hirohito Yamazaki, Shinji Nakao, Yu Seiki, Kanako Mochizuki, Chizuru Saito
Publikováno v:
European Journal of Haematology. 95(3):230-238
Trisomy 8 (+8), one of the most common chromosomal abnormalities found in patients with myelodysplastic syndromes (MDS), is occasionally seen in patients with otherwise typical aplastic anemia (AA). Although some studies have indicated that the prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dacd7ff924665cd0712492b566cde846
http://hdl.handle.net/2297/43415
http://hdl.handle.net/2297/43415
Autor:
Yumi Sasaki, Shinji Nakao, Akiyoshi Takami, Kohei Hosokawa, Naomi Sugimori, Hirohito Yamazaki, Yu Seiki, Chizuru Saito
Publikováno v:
Haematologica. 98(6):901-907
Although myelodysplastic syndromes are heterogeneous disorders comprising a benign subset of bone marrow failure similar to aplastic anemia, no laboratory test has been established to distinguish it from bone marrow failures that can evolve into acut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5eb1974f5bcaf0f56c7e6a7bcf4959b
http://hdl.handle.net/2297/35212
http://hdl.handle.net/2297/35212
Autor:
Yu Seiki, Seishi Ogawa, Kohei Hosokawa, Naomi Sugimori, Ken Ishiyama, Yumi Sasaki, Takamasa Katagiri, Shinji Nakao, Aiko Sato-Otsubo, Masashi Sanada
Publikováno v:
Haematologica. 97:1845-1849
To characterize bone marrow failure with del(13q), we reviewed clinical records of 22 bone marrow failure patients possessing del(13q) alone or del(13q) plus other abnormalities. All del(13q) patients were diagnosed with myelodysplastic syndrome-uncl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::991eab8d4324ee67b06eeb0ffa7cfab9
https://doi.org/10.3324/haematol.2011.061127
https://doi.org/10.3324/haematol.2011.061127
Autor:
Takamasa Katagiri, Kohei Hosokawa, Takashi Nakakuki, Mariko Okada-Hatakeyama, Shinji Nakao, Hiroshi Kawamoto, Shigeki Ohtake, Ken Ishiyama, Yu Seiki
Publikováno v:
Stem cells (Dayton, Ohio). 31(3)
Mutation of the phosphatidylinositol N-acetylglucosaminyltransferase subunit A (PIG-A) gene in hematopoietic stem cells (HSCs) results in the loss of glycosylphosphatidylinositol-anchored proteins (GPI-APs) on HSCs, but minimally affects their develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::853914b708c6a1864c6c968655f0e6f2
https://pubmed.ncbi.nlm.nih.gov/23316019
https://pubmed.ncbi.nlm.nih.gov/23316019
Autor:
Yumi Sasaki, Takamasa Katagiri, Yu Seiki, Chizuru Saito, Yasuhiko Yamamoto, Shinji Nakao, Kohei Hosokawa, Luis J. Espinoza, Hirohito Yamazaki
Publikováno v:
Blood. 120:4399-4399
Abstract 4399 Background: An increase in glycosylphosphatidylinositol-anchored protein-deficient (GPI-AP−) blood cells is a significant predictor of a good response to immunosuppressive therapy in patients with aplastic anemia (AA) and low-risk mye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85a42501b8e5f767bd703d4b0ad128b7
https://doi.org/10.1182/blood.v120.21.4399.4399
https://doi.org/10.1182/blood.v120.21.4399.4399
Autor:
Shinji Nakao, Ken Ishiyama, Yu Seiki, Aiko Sato-Otsubo, Masashi Sanada, Kohei Hosokawa, Naomi Sugimori, Seishi Ogawa, Yumi Sasaki, Takamasa Katagiri
Publikováno v:
Blood. 118:3420-3420
Abstract 3420 Background: Numerical karyotypic abnormalities such as −7/del(7q) and del(13q) are occasionally seen in patients with bone marrow (BM) failure who do not have typical signs of myelodysplasia. The WHO 2008 defined this subset of BM fai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e766ec24141520ba4aeb658dd803989e
https://doi.org/10.1182/blood.v118.21.3420.3420
https://doi.org/10.1182/blood.v118.21.3420.3420